Canonical Allele Identifier: PA2825607753
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 3102824
ClinVar RCV Id: RCV004396214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120926.1:p.Thr251Ile
CA4191352
NM_001127454.2:c.752C>T